Isomer selective synthesis of methanofullerenes

ABSTRACT

[6,6]-Phenyl C 71  butyric acid derivatives (C 70 -PCBR 3 ) having a selectivity of greater than 95 wt % of the α-isomer are provided by reacting fullerene C 70  with a dialkyl sulfonium tetrafluoroborate having the formula:

RELATED APPLICATIONS

This application is a continuation in part application of co-pending application Ser. No. 15/073,335, filed Mar. 17, 2016, entitled ISOMER-SELECTIVE SYNTHESIS OF METHANOFULLERENES, the contents of which are incorporated in its entirety.

FIELD OF THE INVENTION

The invention addresses the synthesis of specific isomers of methano-adducts of C70 and higher fullerenes.

BACKGROUND OF THE INVENTION

Methanofullerenes such as phenyl-C₆₁-butyric acid methyl ester (PC₆₀BM) and phenyl-C₇₁-butyric acid methyl ester (PC₇₀BM) are widely used as electron acceptor materials in organic photovoltaic devices (OPV) and organic photodetectors (OPD) (G. Dennler et al., Adv. Mater. 2009, 21, 1-16; F. He and L. Yu., J. Phys. Chem. Lett. 2011, 2, 3102-3113; I. Etxebarria et al., Journal of Photonics for Energy 2015, 5, 057214).

The synthesis of methanofullerenes is most commonly based on [3+2] cycloadditions by the reaction of diazomethanes, diazoacetates, diazoamides or diazoketones (A. Hirsch and M. Brettreich, Fullerenes: Chemistry and Reactions, 2005, Wiley-VCH, ISBN: 3-527-60820-2, pp. 119ff). Also, cyclopropanation reactions by nucleophilic addition of deprotonated α-halo-esters or ketones have been used successfully (C. Bingel, Chem. Ber. 1993, 126, 1957-1959). It has been demonstrated that addition of unsymmetrically substituted diazoalkanes leads to two isomers, i.e., [5,6]fulleroids having an open C—C bond on the fullerene cage and [6,6]methanofullerenes (Hummelen et al., J. Org. Chem. 1995, 60, 532-538). While fulleroids are formed first, when submitted to heat or irradiation by light they convert quantitative to the latter, resulting in [6,6]methanofullerenes as the thermodynamically stable compound used for OPV and OPD applications (Hummelen et al., J. Org. Chem. 1995, 60, 532-538) (Kooistra et al., Org. Lett. 2007, 9, 551-554). An additional degree of complexity is reached when C₇₀ instead of C₆₀ is the reactant. Whereas C₆₀ contains only one type of 6-6 bond (a bond between two six membered rings), C₇₀ has four, leading to mixtures of regioisomers. Even larger numbers of different regioisomers are formed in the case of multiple (such as bis- and tris-) adducts. A general discussion of isomers among fullerene adducts in the case of fullerene larger than C₆₀ (such as C₇₀, C₇₆, C₇₈ and C₈₄) can be found in Thilgen et al. (Angew. Chem. Int. Ed. Engl. 1997, 36, 2268-2280.). A more specific description of isomers of phenyl-C₇₁-butyric acid methyl ester (PC₇₀BM) has been provided by Wienk et al. (Angew. Chem. Int. Ed. 2003, 42, 3371-3375, U.S. Pat. No. 7,906,797 B2, U.S. Pat. No. 8,481,996 B2). Using a [3+2] cycloaddition of substituted diazomethane (using tosylhydrazone as reactant), products were analyzed using ¹H NMR and ¹³C NMR. It was concluded that the major isomer (˜85%) is the α-type compound formed by 1,3-dipolar addition to the most “polar” double bond (the C(8)-C(25) bond) yielding a chiral enantiomeric mixture. Two minor isomers (a combined proportion of ˜15%) were also identified as achiral stereoisomeric “type” addends, in which the addend is bound to the C(9)-C(10) double bond (the second most “polar” C═C bond in the C₇₀ skeleton, after the C(8)-C(25) bond). For simplification, in this document, it will not be differentiated between the enantiomers of the α-isomer, which are referred to collectively as the “α-isomer” or “α-PC₇₀BM.” Similarly, the two achiral isomers are not addressed individually, and they are collectively referred to as the “β-isomers” or “β-PC₇₀BM.” The chromatographic separation of these isomers has been found to be extremely challenging and no viable preparative solution exists.

Reactions of semistabilized sulfur ylides generated in situ from corresponding sulfonium salts with C₇₀ have been investigated. Such synthetic approach has been initially reported by Ito et al. (Synlett. 2013, 24, 1988-1992; JP2014-034519A), who prepared dimethyl (5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate by bromination of methyl 5-phenylpentanoate at the benzyl position, followed by nucleophilic substitution of the bromide with dimethyl sulfide. After optimization of the reaction with C₆₀ resulting in [6,6]-Phenyl-C₆₁-butyric acid methyl ester (PC₆₀BM) without initial formation of the [5,6] isomer, the reaction was carried out with C₇₀, in o-dichlorobenzene (ODCB). [6,6] PC₇₀BM was obtained with 45% isolated yield and the products consisted of the same isomers having a similar component ratio (e.g., α:β 85:15) as in the conventional substituted diazoalkane addition approach by Wienk et al. (Angew. Chem. Int. Ed. 2003, 42, 3371-3375, U.S. Pat. No. 7,906,797 B2, U.S. Pat. No. 8,481,996 B2), e.g., 85:15.

While the reaction of C₇₀ with dimethyl (5-methoxy-5-oxo-1-phenylpentyl) sulfonium salt resulted in an isomeric mixture, reactions of dimethyl-sulfonium ylides with C₇₀ produced methanofullerenes of the type C₇₀CHCOR with regioselectivity (Wang et al., J. Org. Chem. 1996, 61, 5198-5199). In yet other instances, using the methyl-, iso-propyl-substituted sulfonium ylide of methyl 5-phenylpentanoate resulted in enrichment of α-PC₇₀BM to 95% (based on ¹H NMR spectroscopy)(JP2014-034519A).

No systematic correlation of the structure of the substituted sulfonium ylide and the extent of regioselectivity has been established.

SUMMARY

The regioselective synthesis of α-PC₇₀BR₃ is achieved by reaction of di-alkyl sulfonium salts (1) with C₇₀. Di-alkyl-(5-alkoxy-5-oxo-1-phenylpentyl) sulfonium salts I used for the isomer-selective synthesis of phenyl-C₇₁-butyric acid alkyl esters (PC₇₀BR₃) includes:

where R₁ and R₂ are independently —CR₄R₅R₆;

where R₄, R₅, and R₆ are independently selected from H, or C₁-C₁₂ alkyl; where for any one of R₁ and R₂ no more than one of R₄, R₅, and R₆ can be H;

where R₃ is independently selected from H, optionally substituted C1-C12 aliphatic wherein one or more carbon units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or —NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl;

where R_(a) is independently selected from H, optionally substituted C1-C6 aliphatic; optionally substituted C3-C6 cycloaliphatic or optionally substituted phenyl;

where X is an anion selected from Br⁻, I⁻, Cl⁻, F⁻, BF₄ ⁻, PF₆ ⁻, SbF₆ ⁻, AsF₆ ⁻, OSO₂CH₃ ⁻, OSO₂CF₃ ⁻, OSO₂C₄F₉ ⁻, OSO₂OCH₃ ⁻, OCOCH₃ ⁻, OCOCF₃ ⁻, OSO₂(C₆H₄)CH₃ ⁻, OSO₂(C₆H₄)CF₃ ⁻, N(SO₂CF₃)₂ ⁻, OSO₂CH₂CH₂CH₂CH₂SO₂O⁻, OH⁻, I₃ ⁻, N(CN)₂ ⁻, 7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonate, B(C₆H₅)₄ ⁻ or OSO₂OH⁻.

In one or more embodiments, the regioselective synthesis of α-PC₇₀BR₃ is achieved by reaction of di-alkyl sulfonium salts (1) with C₇₀.

where R₁ and R₂ are independently —CR₄R₅R₆;

R₄, R₅, and R₆ are independently selected from H, or C1-C12 alkyl;

wherein for any one of R₁ and R₂ no more than one of R₄, R₅, and R₆ can be H;

wherein R₃ is independently selected from H and C1-C12 alkyl; and

wherein X is an anion selected from Br⁻, I⁻, Cl⁻, F⁻, BF₄ ⁻, PF₆ ⁻, SbF₆ ⁻, AsF₆ ⁻, OSO₂CH₃ ⁻, OSO₂CF₃ ⁻, OSO₂C₄F₉ ⁻, OSO₂OCH₃ ⁻, OCOCH₃ ⁻, OCOCF₃—, OSO₂(C₆H₄)CH₃ ⁻, OSO₂(C₆H₄)CF₃ ⁻, N(SO₂CF₃)₂ ⁻, OSO₂CH₂CH₂CH₂CH₂SO₂O⁻, OH⁻, I₃ ⁻, N(CN)₂ ⁻, 7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonate, B(C₆H₅)₄ ⁻ or OSO₂OH⁻.

In one or more embodiments one of R₄, R₅, and R₆ is H.

In one or more embodiments R₁ and R₂ are both iso-propyl.

In one or more embodiments R₁ and R₂ are both sec-butyl.

In one or more embodiments R₁ is iso-propyl and R₂ is sec-butyl.

In one or more embodiments R₃ is selected from H and C1-C12 alkyl.

In one or more embodiments R₃ is branched or straight C1-C6 alkyl.

In one or more embodiments R₃ is branched or straight C6 alkyl.

In one or more embodiments wherein R₃ is n-hexyl.

In one or more embodiments one or more carbon units, including terminal carbon, are optionally and independently replaced by —O—.

In one or more embodiments R₃ is a glycolyl.

In one or more embodiments, R₃ is a polyglycolyl group with terminal OH group being optionally replaced by alkyl or alkoxy.

In one or more embodiments X is BF₄ ⁻.

In one or more embodiments the reaction provides greater than 97.5% selectivity of the α-isomer.

In one or more embodiments the reaction provides greater than 98 wt % selectivity of the α-isomer.

In one or more embodiments reacting includes reacting the fullerene C₇₀ and the dialkyl sulfonium tetrafluoroborate in the presence of a base.

In one or more embodiments the base comprises an organic base.

In one or more embodiments the base includes 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).

In another aspect, [6,6]-Phenyl C₇₁ butyric acid methyl ester (C₇₀-PCBR₃) comprising greater than 98% of the α-isomer is provided, wherein R₃ is selected from H, optionally substituted C1-C12 aliphatic wherein one or more carbon units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or —NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl. No post-synthesis enhancement of isomer is required.

In another aspect, [6,6]-Phenyl C₇₁ butyric acid methyl ester (C₇₀-PCBR₃) comprising greater than 99% of the α-isomer is provided, wherein R₃ is selected from H, optionally substituted C1-C12 aliphatic wherein one or more carbon units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or —NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl. No post-synthesis enhancement of isomer is required.

In one or more embodiments, the [6,6]-Phenyl C₇₁ butyric acid alkyl derivative is [6,6]-Phenyl C₇₁ butyric acid methyl ester.

In one or more embodiments, the reaction provides greater than 95% of the α-isomer.

In one or more embodiments, the reaction provides greater than 98 wt/o of the α-isomer.

In one or more embodiments, R₁ is iso-propyl, and/or R₂ is iso-propyl.

In one or more embodiments, R₁ and/or R₂ is sec-butyl.

In one or more embodiments, R₁ and/or R₂ is tert-butyl.

In one or more embodiments, R₅ is H.

In one or more embodiments, the method further includes reacting the fullerene C₇₀ and the dialkyl sulfonium tetrafluoroborate in the presence of a base.

In one or more embodiments, the base is an organic base.

In one or more embodiments, the base includes 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).

In one or more embodiments, the regioselective synthesis of α-PC₇₀BM is achieved by reaction of di-alkyl sulfonium salts tetrafluoroborates (Ia) with C₇₀.

where R₁ and R₂ are independently —CR₄R₅R₆;

R₄, R₅, and R₆ are independently selected from H, or C₁-C₁₃ alkyl;

wherein for any one of R₁ and R₂ no more than one of R₄, R₅, and R₆ can be H.

In one or more embodiments, the reaction provides [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) comprising greater than 95% of the α-isomer.

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having greater than 97% of the α-isomer

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having greater than 98% of the α-isomer

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having greater than 99% of the α-isomer.

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having greater than 99.5% of the α-isomer.

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having greater than 99.9% of the α-isomer.

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having 97-99.9% of the α-isomer.

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having 98-99.5% of the α-isomer.

In one or more embodiments, [6,6]-Phenyl C₇₁ butyric acid alkyl ester (C70-PCBR₃) is provided having greater than 97-99% of the α-isomer. The high α-isomer content is achieved by isomer-selective synthesis, without enhancement by separation or removal of the β-isomer.

As used herein the term “aliphatic” encompasses the terms alkyl, alkenyl, alkynyl, each of which being optionally substituted as set forth below.

As used herein, an “alkyl” group refers to a saturated aliphatic hydrocarbon group containing 1-12 (e.g., 1-8, 1-6, or 1-4) carbon atoms. In other embodiments, “alkyl” is a linear, cyclic or branched, saturated or unsaturated hydrocarbon. An alkyl group can be straight or branched. Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-heptyl, or 2-ethylhexyl. An alkyl group can be substituted (i.e., optionally substituted) with one or more substituents such as halo, phospho, cycloaliphatic [e.g., cycloalkyl or cycloalkenyl], heterocycloaliphatic [e.g., heterocycloalkyl or heterocycloalkenyl], aryl, heteroaryl, alkoxy, aroyl, heteroaroyl, acyl [e.g., (aliphatic)carbonyl, (cycloaliphatic)carbonyl, or (heterocycloaliphatic)carbonyl], nitro, cyano, amido [e.g., (cycloalkylalkyl)carbonylamino, arylcarbonylamino, aralkylcarbonylamino, (heterocycloalkyl)carbonylamino, (heterocycloalkylalkyl)carbonylamino, heteroarylcarbonylamino, heteroaralkylcarbonylamino alkylaminocarbonyl, cycloalkylaminocarbonyl, heterocycloalkylaminocarbonyl, arylaminocarbonyl, or heteroarylaminocarbonyl], amino [e.g., aliphaticamino, cycloaliphaticamino, or heterocycloaliphaticamino], sulfonyl [e.g., aliphatic-SO₂], sulfinyl, sulfanyl, sulfoxy, urea, thiourea, sulfamoyl, sulfamide, oxo, carboxy, carbamoyl, cycloaliphaticoxy, heterocycloaliphaticoxy, aryloxy, heteroaryloxy, aralkyloxy, heteroarylalkoxy, alkoxycarbonyl, alkylcarbonyloxy, or hydroxy. Without limitation, some examples of substituted alkyls include carboxyalkyl (such as HOOCalkyl, alkoxycarbonylalkyl, and alkylcarbonyloxyalkyl), cyanoalkyl, hydroxyalkyl, alkoxyalkyl, acylalkyl, aralkyl, (alkoxyaryl)alkyl, (sulfonylamino)alkyl (such as (alkyl-SO₂-amino)alkyl), aminoalkyl, amidoalkyl, (cycloaliphatic)alkyl, or haloalkyl.

As used herein, an “alkenyl” group refers to an aliphatic carbon group that contains 2-12 (e.g., 2-12, 2-6, or 2-4) carbon atoms and at least one double bond. Like an alkyl group, an alkenyl group can be straight or branched. Examples of an alkenyl group include, but are not limited to allyl, isoprenyl, 2-butenyl, and 2-hexenyl. An alkenyl group can be optionally substituted with one or more substituents such as halo, phospho, cycloaliphatic [e.g., cycloalkyl or cycloalkenyl], heterocycloaliphatic [e.g., heterocycloalkyl or heterocycloalkenyl], aryl, heteroaryl, alkoxy, aroyl, heteroaroyl, acyl [e.g., (aliphatic) carbonyl, (cycloaliphatic)carbonyl, or (heterocycloaliphatic) carbonyl], nitro, cyano, amido [e.g., (cycloalkylalkyl) carbonylamino, arylcarbonylamino, aralkylcarbonylamino, (heterocycloalkyl)carbonylamino, (heterocycloalkylalkyl)carbonylamino, heteroarylcarbonylamino, heteroaralkylcarbonylamino alkylaminocarbonyl, cycloalkylaminocarbonyl, heterocycloalkylaminocarbonyl, arylaminocarbonyl, or heteroarylaminocarbonyl,] amino [e.g., aliphaticamino, cycloaliphaticamino, heterocycloaliphaticamino, or aliphaticsulfonylamino], sulfonyl [e.g., alkyl-SO₂, cycloaliphatic-SO₂, or aryl-SO₂], sulfinyl, sulfanyl, sulfoxy, urea, thiourea, sulfamoyl, sulfamide, oxo, carboxy, carbamoyl, cycloaliphaticoxy, heterocycloaliphaticoxy, aryloxy, heteroaryloxy, aralkyloxy, heteroaralkoxy, alkoxycarbonyl, alkylcarbonyloxy, or hydroxy.

As used herein, an “alkynyl” group refers to an aliphatic carbon group that contains 2-12 (e.g., 2-12, 2-6, or 2-4) carbon atoms and has at least one triple bond. An alkynyl group can be straight or branched. Examples of an alkynyl group include, but are not limited to, propargyl and butynyl. An alkynyl group can be optionally substituted with one or more substituents such as aroyl, heteroaroyl, alkoxy, cycloalkyloxy, heterocycloalkyloxy, aryloxy, heteroaryloxy, aralkyloxy, nitro, carboxy, cyano, halo, hydroxy, sulfo, mercapto, sulfanyl [e.g., aliphaticsulfanyl or cycloaliphaticsulfanyl], sulfinyl [e.g., aliphaticsulfinyl or cycloaliphaticsulfinyl], sulfonyl [e.g., aliphatic-SO₂, aliphaticamino-SO₂, or cycloaliphatic-SO₂], amido [e.g., aminocarbonyl, alkylaminocarbonyl, alkylcarbonylamino, cycloalkylaminocarbonyl, heterocycloalkylaminocarbonyl, cycloalkylcarbonylamino, arylaminocarbonyl, arylcarbonylamino, aralkylcarbonylamino, (heterocycloalkyl)carbonylamino, (cycloalkylalkyl)carbonylamino, heteroaralkylcarbonylamino, heteroarylcarbonylamino or heteroarylaminocarbonyl], urea, thiourea, sulfamoyl, sulfamide, alkoxycarbonyl, alkylcarbonyloxy, cycloaliphatic, heterocycloaliphatic, aryl, heteroaryl, acyl [e.g., (cycloaliphatic)carbonyl or (heterocycloaliphatic) carbonyl], amino [e.g., aliphaticamino], sulfoxy, oxo, carboxy, carbamoyl, (cycloaliphatic)oxy, (heterocycloaliphatic) oxy, or (heteroaryl)alkoxy.

As used herein, a “cycloaliphatic” group encompasses a “cycloalkyl” group and a “cycloalkenyl” group, each of which being optionally substituted as set forth below.

As used herein, a “cycloalkyl” group refers to a saturated carbocyclic mono- or bicyclic (fused or bridged) ring of 3-10 (e.g., 5-10) carbon atoms. Examples of cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, norbornyl, cubyl, octahydro-indenyl, decahydro-naphthyl, bicyclo[3.2.1]octyl, bicyclo[2.2.2] octyl, bicyclo[3.3.1]nonyl, bicyclo[3.3.2.]decyl, bicycle [2.2.2]octyl, adamantyl, or ((aminocarbonyl)cycloalkyl) cycloalkyl.

A “cycloalkenyl” group, as used herein, refers to a nonaromatic carbocyclic ring of 3-12 (e.g., 4-8) carbon atoms having one or more double bonds. Examples of cycloalkenyl groups include cyclopentenyl, 1,4-cyclohexa-di-enyl, cycloheptenyl, cyclooctenyl, hexahydro-indenyl, octahydronaphthyl, cyclohexenyl, cyclopentenyl, bicyclo[2.2.2]octenyl, or bicyclo [3.3.1]nonenyl.

A cycloalkyl or cycloalkenyl group can be optionally substituted with one or more substituents such as phosphor, aliphatic [e.g., alkyl, alkenyl, or alkynyl], cycloaliphatic, (cycloaliphatic) aliphatic, heterocycloaliphatic, (heterocycloaliphatic) aliphatic, aryl, heteroaryl, alkoxy, (cycloaliphatic) oxy, (heterocycloaliphatic)oxy, aryloxy, heteroaryloxy, (araliphatic)oxy, (heteroaraliphatic)oxy, aroyl, heteroaroyl, amino, amido [e.g., (aliphatic)carbonylamino, (cycloaliphatic)carbonylamino, ((cycloaliphatic)aliphatic) carbonylamino, (aryl)carbonylamino, (araliphatic)carbonylamino, (heterocycloaliphatic)carbonylamino, ((heterocycloaliphatic) aliphatic)carbonylamino, (heteroaryl) carbonylamino, or (heteroaraliphatic)carbonylamino], nitro, carboxy [e.g., HOOC, alkoxycarbonyl, or alkylcarbonyloxy], acyl [e.g., (cycloaliphatic)carbonyl, ((cycloaliphatic) aliphatic)carbonyl, (araliphatic)carbonyl, (heterocycloaliphatic) carbonyl, ((heterocycloaliphatic)aliphatic)carbonyl, or (heteroaraliphatic)carbonyl], cyano, halo, hydroxy, mercapto, sulfonyl [e.g., alkyl-SO₂ and aryl-SO₂, sulfinyl [e.g., alkyl-S(O)] sulfanyl [e.g., alkyl-S], sulfoxy, urea, thiourea, sulfamoyl, sulfamide, oxo, or carbamoyl.

As used herein, an “aryl” group used alone or as part of a larger moiety as in “aralkyl”, “aralkoxy”, or “aryloxyalkyl” refers to C6-C12 monocyclic (e.g., phenyl); bicyclic (e.g., indenyl, naphthalenyl, tetrahydronaphthyl, tetrahydroindenyl); and tricyclic (e.g., fluorenyl tetrahydxofluorenyl, or tetrahydxoanthracenyl, anthracenyl) ring systems in which the monocyclic ring system is aromatic or at least one of the rings in a bicyclic or tricyclic ring system is aromatic. The bicyclic and tricyclic groups include benzofused 2-3 membered carbocyclic rings. For example, a benzofused group includes phenyl fused with two or more C4-C8 carbocyclic moieties. An aryl is optionally substituted with one or more substituents including aliphatic [e.g., alkyl, alkenyl, or alkynyl]; cycloaliphatic; (cycloaliphatic) aliphatic; heterocycloaliphatic; (heterocycloaliphatic) aliphatic; aryl; heteroaryl; alkoxy; (cycloaliphatic) oxy; (heterocycloaliphatic)oxy; aryloxy; heteroaryloxy; (araliphatic)oxy; (heteroaraliphatic)oxy; aroyl; heteroaroyl; amino; oxo (on a non-aromatic carbocyclic ring of a benzofused bicyclic or tricyclic aryl); nitro; carboxy; amido; acyl [e.g., (aliphatic)carbonyl; (cycloaliphatic) carbonyl; ((cycloaliphatic)aliphatic)carbonyl; (araliphatic)carbonyl; (heterocycloaliphatic)carbonyl; ((heterocycloaliphatic) aliphatic)carbonyl; or (heteroaraliphatic) carbonyl]; sulfonyl [e.g., aliphatic-SO₂ or amino-SO₂; sulfinyl [e.g., aliphatic-S(O) or cycloaliphatic-S(O)]; sulfanyl [e.g., aliphatic-S]; cyano; halo; hydroxy; mercapto; sulfoxy; urea; thiourea; sulfamoyl; sulfamide; or carbamoyl. Alternatively, an aryl can be unsubstituted.

BRIEF DESCRIPTION OF THE DRAWING

The invention is described with reference to the following figures, which are presented for the purpose of illustration only and are not intended to be limiting of the invention.

FIG. 1 is an ¹H NMR of a concentrated sample (30 mg/mL) of α-PC₇₀BM in deuterated chloroform showing the full spectrum (above) and an enlarged view of trace region in the box (below), illustrating the presence of α-PC₇₀BM (3.65 ppm) and the β-PC₇₀BM impurity (3.72 ppm and 3.48 ppm). The abundance of α-PC₇₀BM is measured here to be 98.1% (3.65 ppm+3.89 ppm+3.40 ppm) taking into account the satellites signals for the α-PC₇₀BM methyl singlet (3.89 ppm and 3.40 ppm, indicating the natural occurrence of ¹³C).

FIG. 2 is an analytical HPLC chromatograph overlay of PC₇₀BM samples made using a range of precursors, in which the leading shoulder is 3-PC₇₀BM and the main signal is α-PC₇₀BM (Cosmosil Buckyprep material was used as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene was used as the mobile phase at 1 mL/min.).

FIG. 3 is a ¹H NMR spectrum of mixed PC₇₁BC6 using conventional tosylhydrazone method (upper trace) and α-PC₇₁BC6 using sulfonium reagent (lower trace) according to one or more embodiment of the invention.

FIG. 4 is an analytical HPLC chromatograph overlay of mixed PC₇₀BC6 using conventional tosylhydrazone method (upper trace 400) and α-PC₇₀BC6 using sulfonium reagent (lower trace 410) according to one or more embodiment of the invention. The leading shoulder is β-PC₇₀BC6 and the main signal is α-PC₇₀BC6 (Cosmosil Buckyprep material was used as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene was used as the mobile phase at 1 mL/min.).

FIG. 5 is an expanded view of ¹H NMR spectrum of FIG. 3 between 4.2-3.8 ppm of mixed PC₇₀BC6 using conventional tosylhydrazone method (upper trace) and α-PC₇₀BC6 using sulfonium reagent (lower trace) according to one or more embodiment of the invention.

DETAILED DESCRIPTION

Di-alkyl-(5-alkoxy-5-oxo-1-phenylpentyl) sulfonium salts I is used for the isomer-selective synthesis of phenyl-C₇₁-butyric acid alkyl esters (PC₇₀BR₃).

where R₁ and R₂ are independently —CR₄R₅R₆;

R₄, R₅, and R₆ are independently selected from H, or C₁-C₁₂ alkyl;

wherein for any one of R₁ and R₂ no more than one of R₄, R₅, and R₆ can be H;

wherein R₃ is independently selected from H, optionally substituted branched or straight C1-C12 aliphatic wherein one or more carbon units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or —NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl;

where R_(a) is independently selected from H, optionally substituted C1-C6 aliphatic; optionally substituted C3-C6 cycloaliphatic or optionally substituted phenyl; and

wherein X is an anion selected from Br⁻, I⁻, Cl⁻, F⁻, BF₄ ⁻, PF₆ ⁻, SbF₆ ⁻, AsF₆ ⁻, OSO₂CH₃ ⁻, OSO₂CF₃ ⁻, OSO₂C₄F₉ ⁻, OSO₂OCH₃ ⁻, OCOCH₃ ⁻, OCOCF₃ ⁻, OSO₂(C₆H₄)CH₃ ⁻, OSO₂(C₆H₄)CF₃ ⁻, N(SO₂CF₃)₂ ⁻, OSO₂CH₂CH₂CH₂CH₂SO₂O⁻, OH⁻, I₃ ⁻, N(CN)₂ ⁻, 7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonate, B(C₆H₅)₄ ⁻ or OSO₂OH⁻.

In one or more embodiments, R₃ can be an alkyl ester from C₁ to C₁₂, while R₁ and R₂ are independently —CR₄R₅R₆ with R₄, R₅, and R₆ being independently selected from H or C₁ to C₁₂ alkyl. For any one of R₁ and R₂ no more than one of R₄, R₅, and R₆ can be H. In exemplary embodiments, R₁ and R₂ can be independently selected from iso-propyl (R₄=R₅=Me and R₆=H), sec-butyl (R₄=Me, R₅=Et and R₆=H), t-butyl (R₄=R₅=R₆=Me), i-pentyl (R₄=R₅=Me and R₆=Et), penta-3-yl (R₄=R₅=Et and R₆=H), hexa-2-yl (R₄=Me, R₅=Bu and R₆=H), hexa-3-yl (R₄=Et, R₅=Pr and R₆=H), 2-methylpenta-2-yl (R₄=R₅=Me and R₆=Pr), 3-methylpenta-3-yl (R₄=R₅=Et and R₆=Me), and 2, 3-dimethylbutan-2-yl (R₄=R₅=Me and R₆=i-Pr), where Me is methyl, Et is ethyl and Pr is propyl. In a particular embodiment, R₁ and R₂ are both iso-propyl. In a particular embodiment, R₁ is iso-propyl and R₂ is sec-butyl. In a particular embodiment, R₁ and R₂ are both sec-butyl.

In one or more embodiments, R₃ includes methyl.

In one or more embodiments, the di-alkyl-(5-alkoxy-5-oxo-1-phenylpentyl) can be compound Ia.

where R₁ and R₂ are independently —CR₄R₅R₆;

R₄, R₅, and R₆ are independently selected from H, or C₁-C₁₃ alkyl;

wherein for any one of R₁ and R₂ no more than one of R₄, R₅, and R₆ can be H.

In exemplary embodiments, R₁ and R₂ can be independently selected from i-propyl (R₄=R₅=Me and R₆=H), sec-butyl (R₄=Me, R₅=Et and R₆=H), t-butyl (R₄=R₅=R₆=Me), i-pentyl (R₄=R₅=Me and R₆=Et), penta-3-yl (R₄=R₅=Et and R₆=H), hexa-2-yl (R₄=Me, R₅=Bu and R₆=H), hexa-3-yl (R₄=Et, R₅=Pr and R₆=H), 2-methylpenta-2-yl (R₄=R₅=Me and R₆=Pr), 3-methylpenta-3-yl (R₄=R₅=Et and R₆=Me), and 2, 3-dimethylbutan-2-yl (R₄=R₅=Me and R₆=i-Pr). In one or more embodiments, the di-alkyl-(5-alkoxy-5-oxo-1-phenylpentyl) can be compound Ia.

where R₁ and R₂ are iso-propyl.

In one or more embodiments, R₁ and R₂ are iso-propyl are preferred groups. Isopropyl has been identified as a substituent that provides enhanced isomer enrichment of the α-PC₇₀BR₃ product. Enhanced α-PC₇₀BR₃ can be obtained for a range of R₃ groups using Compound Ia.

In one or more embodiments R₃ is selected to impart desirable properties in the α-PC₇₀BR₃ product. For example, R₃ is selected for α-PC₇₀BR₃ products having enhanced photoactive properties, such as improved electron-accepting or -donating properties. In such embodiments, short chain alkyl groups can be used. In one or more embodiments, wherein R₃ is independently selected from H and C1-C12 aliphatic. In one or more embodiments, wherein R₃ is independently selected from H and C1-C12 alkyl. In one or more embodiments, wherein R₃ is C1-C6 alkyl. In one or more embodiments, wherein R₃ is C6 alkyl.

In other examples, R₃ can be selected to improve solubility of the product α-PC₇₀BR₃ and to tailor the product α-PC₇₀BR₃ for improved solubility in selected solvents. Thus, where it is desirable to improve solubility in aromatic solvents, R₃ can be an optionally substituted alkyl groups (particularly C6 and higher).

In other embodiments, where it is desirable to improve solubility in polar solvents, R₃ can be aliphatic or cycloaliphatic groups in which polar substituents are inserted in the R₃ backbone or as substituents.

In one or more embodiments, R₃ is optionally substituted branched or straight C1-C12 aliphatic wherein one or more carbon units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, pyridinyl or —NR_(a)—.

In one or more embodiments, R₃ is optionally substituted branched or straight C1-C12 alkyl wherein one or more CH₂ units, including the terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, pyridinyl or —NR_(a)—.

In one or more embodiments, R₃ is optionally substituted branched or straight C1-C12 alkyl wherein one or more CH₂ units, including the terminal carbon, are replaced by —O—.

In one or more embodiments, in order to improve solubility in water and other polar solvents such as alcohols including but not limited to methanol, ethanol, n- and i-propanol, R₃ is a polyglycolyl group with terminal OH group being optionally replaced by alkyl or alkoxy. Polyglycolyl groups include but are not limited to polyethylene glycolyl and polypropylene glycolyl containing between 2 and 100 monomer units with 2 to 12 being preferred.

A synthetic path targeting selectively α-PC₇₀BR₃ (where R₃ is as described above) and specifically α-PC₇₀BM (where M is methyl) has been developed. In one or more embodiments, reaction of C₇₀ with sulfonium salts of the formula I and Ia provide α-PC₇₀BR₃ (where R₃ is as described above) and specifically α-PC₇₀BM with a selectivity of greater than 95%, 97% or higher, 98% or higher, 99% or higher, 99.5% or higher and as high as 99.9%. In one or more embodiments, reaction of C₇₀ with sulfonium salts of the formula I and Ia provide α-PC₇₀BR₃ (where R₃ is as described above) and specifically α-PC₇₀BM with a selectivity bounded by any of the values noted above.

Systematic investigation of the reaction of di-alky-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetraborates with C₇₀ was conducted. The abundance of the different isomers was assessed based on analytical HPLC using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase. For selected experiments, the isomer distribution was also determined by means of peak integration ¹H NMR of purified final products.

Correlations between the identity of the alkyl-groups R₁ and R₂ in di-alkyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborates and the relative abundance of α-PC₇₀BM compared to β-PC₇₀BM were found to be counterintuitive. For example, the α-to-β ratio decreased in changing from iso-propylmethyl- to iso-propylethyl-substitution, while the α-to-β ratio increased in changing from iso-propylethyl- to di-iso-propyl-substitution. While not being bound by any particular mode of operation, it is proposed that the presence of an alkyl substitution at the α-carbon position for both R₁ and R₂ increases the α-isomer selectivity of the reaction.

Di-alkyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborates were synthesized beginning with the bromination of methyl 5-phenylpentanoate followed by nucleophilic substitution of the bromide with the corresponding dialkyl sulfide in presence of silver tetrafluoroborate (Synlett. 2013, 24, 1988-1992.). The detailed experimental procedures are described below for the different examples.

Two different general schemes (Scheme 1 and Scheme 2), shown below, have been demonstrated for the synthesis of di-alkyl-(5-alkoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborates. In addition, other counter ions such as trifluoromethanesulfonate (triflate, CF₃SO₃ ⁻) can be used. Also the use of different leaving groups which may or not become the ion can be envisioned.

“LG”=Leaving Group. “ion”=Counter Ion. “LG” may or may not become “ion”. “Ion” may or may not derive from an additional reagent. In Scheme 1, nucleophilic substitution of the leaving group with dialkyl sulfide provides the desired sulfonium salt.

“LG”=Leaving Group. “Ion”=Counter Ion. “LG₁” can be the same as “LG₂”. “LG₁” can be the same as “Ion”. “LG₂” may or may not become “Ion”. “Ion” may or may not derive from an additional reagent. In Scheme 2, nucleophilic substitution of the leaving group with an alkyl thiol to provide a thioether is followed by reaction with an alkylating reagent (and optionally other reagents) to obtain the desired sulfonium salt.

The leaving groups in Scheme 1 (LG) and 2 (LG1 and LG2) can be selected among —Br, —I, —Cl, —F, —BF₄, —PF₆, —SbF₆, —AsF₆, —OSO₂CH₃, —OSO₂CF₃, —OSO₂C₄F₉, —OSO₂OCH₃, —OCOCH₃, —OCOCF₃, —OSO₂(C₆H₄)CH₃, —OSO₂(C₆H₄)CF₃, —N(SO₂CF₃)₂, —OSO₂CH₂CH₂CH₂CH₂SO₂O—, —OH, —I₃, —N(CN)₂, 7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonate, —B(C₆H₅)₄ and —OSO₂OH. The counter ion (Ion) may be the same as one of leaving groups, except that it bears a negative charge.

The di-alkyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborates used as reactants are given in Table 1, together with the yield of their synthesis. Different from the other reactions, methyl, dodecyl functionalization has been carried out in two subsequent steps as described in JP2014-034519A beginning with the substitution of bromine by S—C₁₂H₂₅.

TABLE 1 Synthesis of Di-alkyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborates Experiment Yield of sulfonium no R1 R2 salt synthesis (%) 1 CH₃ C₁₂H₂₅ 66 (over two steps) 2 CH₃ i-C₃H₇ 37 3 i-C₃H₇ i-C₃H₇ 34 4 C₂H₅ i-C₃H₇ 41 5 C₁₂H₂₅ C₁₂H₂₅ 74

Subsequent reaction of di-alkyl-(5-alkoxy-5-oxo-1-phenylpentyl) sulfonium salts with C₇₀ to provide phenyl-C₇₁-butyric acid alkyl esters (PC₇₀BX) is shown in Scheme 3.

Reaction of di-alkyl-(5-alkoxy-5-oxo-1-phenylpentyl) sulfonium salts with C₇₀ to phenyl-C₇₁-butyric acid alkyl esters (PC₇₀BR₃); “Ion”=Counter Ion.

In one or more embodiments, the reaction is carried out at room temperature (or in slightly elevated temperatures up to ca. 40-50° C.) in presence of base such as DBU (1,8-diazabicyclo[5.4.0]undec-7-ene), DBN (1,5-diazabicyclo[4.3.0]non-5-ene), DABCO (1,4-diazabicyclo(2.2.2)octane), pyridine, 2,6-dimethylpyridine, 2,4,6-trimethylpyridine, DMAP (dimethylaminopyridine), trimethylamine, triethylamine, Hunig's base (N,N-diisopropylethylamine), DMA (dimethylaniline), TMP (2,2,6,6-tetramethylpiperidine), PMP (1,2,2,6,6-pentamethylpiperidine), sodium borohydride, lithium aluminum hydride, sodium hydride, sodium methoxide, lithium methoxide, potassium methoxide, sodium t-butoxide, lithium t-butoxide, potassium t-butoxide, n-butyllithium, t-butyllithium, n-butylmagnesium chloride, t-butylmagnesium chloride, and LiHMDS (lithium hexamethyldisilazide).

In one or more embodiments, the reaction is conducted in an aromatic solvent, such as in o-dichlorobenzene (ODCB).

HPLC chromatograms of [6,6]-Phenyl C₇₁ butyric acid methyl ester produced using the different dialkyl sulfonium salts shown in Table 1 in each of the examples are shown in FIG. 2. In addition, the chromatogram of the product mixture resulting from the currently best established synthesis based on the reaction of tosylhydrazone (a substituted diazoalkane) as described by Hummelen et al. (J. Org. Chem. 1995, 60, 532-538) and Wienk et al. (Angew. Chem. Int. Ed. 2003, 42, 3371-3375, U.S. Pat. No. 7,906,797 B2, U.S. Pat. No. 8,481,996 B2) but using irradiation by light for the isomerization of fulleroid to methanofullerene (Kooistra et al., Org. Lett. 2007, 9, 551-554) is included as curve 600.

Assessing the results of Examples 1c, 2b, 3b, 4b and 5b below (curves 100, 200, 300, 400 and 500, respectively), it can be established that the identity of the alkyl-groups in the di-alkyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborates has an effect on the abundance of α-PC₇₀BM relative to β-PC₇₀BM. The conventional tosylhydrazone route (curve 600) yielded the expected α-to-β ratio of ca. 85:15, similar to that obtained using a di-methyl substituted sulfonium salt (Ito et al., Synlett. 2013, 24, 1988-1992; JP2014-034519A). Surprisingly, when both methyl groups are replaced by the more bulky dodecyl groups, the ratio of the obtained α-PC₇₀BM and β-PC₇₀BM (curve 500) is substantially unaffected. Based on a steric argument one would expect the dodecyl groups to enhance selectivity to produce more α-PC₇₀BM and less β-PC₇₀BM. It is similarly counterintuitive that the product obtained from the methyldodecyl sulfonium salt (curve 100) actually gives less selectivity (more β-PC₇₀BM), despite also being more bulky than the dimethyl sulfonium salt precursor. Investigating sulfonium salts substituted with at least one iso-propyl-substitution, it can be seen in FIG. 2 that the relative amount of β-PC₇₀BM decreases along the trend iso-propylethyl->to i-propylmethyl>di-iso-propyl, when dialkyl sulfonium salts are used in the preparation of C₇₀PCBM. Thus, while the observed change in relative abundance from iso-propylethyl- to iso-propylmethyl sulfonium salts would suggest that decreased steric bulk enhances selectivity, the selectivity surprisingly is improved when di-iso-propyl sulfonium salt (with increased steric bulk) is used in the preparation of C₇₀PCBR₃ compounds.

While the assessment of the relative evolution of the α-to-β ratio by means of HPLC can be considered as being accurate, the determination of absolute values is more difficult, particularly due to incomplete separation of the peaks assigned to α- and β-PC₇₀BM. In an effort to determine the upper limit of the β-PC₇₀BM present, additional analytical HPLC using again a Buckyprep stationary phase but 4:1 cyclohexane:toluene for elution in order to increase the resolution was conducted. Peak integration showed the β-PC₇₀BM being at 1.2%. In order to increase even further the level of confidence of our purity assessment, ¹H NMR using a higher concentration of the analyzed PC₇₀BM (30 mg/mL in CDCl₃) was conducted. The resulting ¹NMR spectrum is given in FIG. 1. FIG. 1 shows the ¹NMR spectrum of a concentrated sample (30 mg/mL) of α-PC₇₀BM (3.65 ppm) in deuterated chloroform. The full spectrum is shown first, followed by a larger image of the area shown in the box. Using the procedure described by Wienk et al. (Angew. Chem. Int. Ed. 2003, 42, 3371-3375), i.e., the integration of the three signals representing methoxy groups (3.48 ppm, 3.65 ppm, and 3.72 ppm, as reported by Wienk et al.) shows an area of ≤1.9% for signals representing β-PC₇₀BM. However, integration of the baseline at different points (for example ˜3.55 ppm and ˜3.33 ppm) shows that the noise in proximity to the 3.65 ppm signal for the α-PC70BM methyl singlet may be artificially inflating the measured abundance of β-PC70BM. We therefore set 1.9% as the upper limit for the abundance of β-PC70BM, however, the actual value can be less.

Integration of ¹H NMR peaks was reported by Wienk et al. (Angew. Chem. Int. Ed. 2003, 42, 3371-3375) to show an abundance of α-PC₇₀BM of approximately 85% in the case of the tosylhydrazone approach whereas, using the same ¹H NMR analysis, reaction of C₇₀ with i-propylmethyl-substituted sulfonium salt resulted in 95.0% of α-PC₇₀BM. Finally, after reaction of di-iso-propyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate with C₇₀ using the conditions described in Example 3b, less than or equal to 1.9% β-PC₇₀BM could be identified my means of the same analytical approach, that is, greater than 98% α-isomer.

The invention is described with reference to the following examples, which are presented for the purpose of illustration only and are not intended to be limiting of the invention.

Example 1a 5-dodecylthio-5-phenylpentanoic acid methyl ester

To a clean, dry 250 mL round bottom flask was added a stir bar and 5.41 g (16.6 mmol, 3 eq) of cesium carbonate. The round bottom was sealed and purged three times with inert gas and vacuum. Anhydrous acetonitrile (27.7 mL) was added to the flask via syringe. The solution was cooled to 0° C., allowed to equilibrate for 15 minutes, and 1-dodecanethiol (3.975 mL, 3.36 g, 16.6 mmol, 3 eq) was added cautiously by syringe. Shortly thereafter, a solution of the bromide (1.5 g, 5.53 mmol, 1 eq) in 5.5 mL of anhydrous acetonitrile was added dropwise (over 30 minutes by syringe pump) with the reaction still at 0° C. Once the addition was complete and an additional 15 minutes had passed, the reaction was allowed to warm to room temperature for 5 hours. The reaction was then filtered and 277 mL of ethyl acetate was added to the filtrate. The organic later was washed with brine 3 times in a separatory funnel, dried with magnesium sulfate, filtered, and solvent was removed by rotary evaporation to give crude product. Silica gel chromatography was used with 9:1 hexane:ethyl acetate as eluent to isolate 1.52 g of the product (an oil which then solidified, 70% yield). ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.35-7.15 (m, 5H), 3.74 (t, J=12.5 Hz, 1H), 3.64 (s, 3H), 2.35-1.1 (m, 28H), 0.88 (t, J=11.0 Hz, 3H).

Example 1b Methyldodecyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate (2)

To a clean, dry 50 mL round bottom flask was added a stir bar and 0.886 g (5.99 mmol, 1.5 eq) of trimethyloxonium tetrafluoroborate. The round bottom was sealed and purged three times with inert gas and vacuum. Anhydrous dichloromethane (6 mL) was added and the mixture was cooled to 0° C. To a second round bottom flask was added the thioether starting material. This flask was also sealed and purged three times with inert gas and vacuum. Anhydrous dichloromethane (10 mL) was added to the second flask by syringe, the thioether starting material was dissolved and the solution was taken back up into the same syringe. The solution containing the thioether starting material was then added dropwise by syringe pump to the flask containing the trimethyloxonium tetrafluoroborate over 30 minutes at 0° C. Once the addition was complete, plus an additional 15 minutes, the reaction was allowed to warm to room temperature for 4.5 hours. Dichloromethane was added and the reaction was extracted twice with water. The DCM layer was dried with magnesium sulfate, filtered, and solvent was removed by rotary evaporation to give 1.805 g (94.8% yield) of product. ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.55-7.4 (m, 5H), 4.97 (t, J=13.0 Hz, 1H), 3.64 (s, 1.5H), 3.63 (s, 1.5H), 3.43 (t, J=13.0 Hz, 1H), 3.26-3.14 (m, 0.5H), 3.04 (s, 1.5H), 2.87-2.74 (m, 0.5H), 2.56 (s, 1.5H), 2.43-1.05 (m, 26H), 0.87 (t, J=11.3 Hz, 3H).

Example 1c [6,6]-Phenyl C₇₁ butyric acid methyl ester

To a clean, dry 250 mL round bottom flask was added a stir bar, 59.3 mg (0.120 mmol, 1 eq) of the sulfonium salt 1, synthesized as described in JP2014-034519A, and 100.8 mg (0.120 mmol, 1 eq) of C₇₀. The round bottom was sealed and purged three times with inert gas and vacuum. 84 mL of ODCB (1,2-dichlorobenzene) anhydrous solvent was added by syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 15 minutes. DBU (1,8-diazabicyclo[5.4.0]undec-7-ene, 0.0179 mL, 0.120 mmol, 1 eq) was added over 5 minutes at 0° C. in 4 mL of anhydrous ODCB via syringe. The reaction was allowed to warm slowly with stirring overnight to room temperature. The abundance of α-PC₇₀BM was qualitatively determined to be <85% based on analytical HPLC using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase.

Example 2a Methyl-i-propyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate (2)

To a clean, dry 50 mL round bottom flask was added a stir bar and 1 g (3.69 mmol, 1 eq) of the bromide. The round bottom was sealed and purged three times with inert gas and vacuum. Dichloromethane (4 mL) and methyl isopropyl sulfide (0.998 g, 1.2 mL, 11.1 mmol, 3 eq) were added to the flask sequentially via syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 15 minutes. Silver tetrafluoroborate (718 mg, 3.69 mmol, 1 eq) was added and the reaction was stirred for 4 hours while warming to room temperature slowly. During this time, the reaction was kept in the dark. Dichloromethane was added and the reaction was extracted twice with water. The DCM layer was dried with magnesium sulfate, filtered, and solvent was removed by rotary evaporation. The crude product was taken up in ethyl acetate and loaded onto a small column which was then flushed with copious ethyl acetate to remove impurities. Product was then eluted with acetone. The acetone was removed by rotary evaporation and a small amount of DCM was added to precipitate silica gel that had come through with the acetone. The DCM was filtered to remove silica gel and once again the solution was rotary evaporated to dryness. 500 mg of product was obtained (37% yield). ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.55-7.4 (m, 5H), 4.92 (t, J=13.0 Hz, 0.5H), 4.82 (t, J=13.0 Hz, 0.5H), 3.94 (septet, J=11.3 Hz, 0.5H), 3.63 (s, 1.5H), 3.62 (s, 1.5H), 3.31 (septet, J=11.5 Hz, 0.5H), 3.01 (s, 1.5H), 3.47 (s, 1.5H), 2.45-2.1 (m, 4H), 1.75-1.4 (m, 2H), 1.65 (d, J=11.5 Hz, 1.5H), 1.57 (d, J=11.5 Hz, 1.5H), 1.40 (d, J=11.5 Hz, 1.5H), 1.28 (d, J=11.5 Hz, 1.5H).

Example 2b [6,6]-Phenyl C₇₁ butyric acid methyl ester

To a clean, dry 250 mL round bottom flask was added a stir bar, 44.2 mg (0.120 mmol, 1 eq) of the sulfonium salt (2), synthesized as described in JP2014-034519A, and 100.8 mg (0.120 mmol, 1 eq) of C₇₀. The round bottom was sealed and purged three times with inert gas and vacuum. 84 mL of ODCB (1,2-dichlorobenzene) anhydrous solvent was added by syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 15 minutes. DBU (1,8-diazabicyclo[5.4.0]undec-7-ene, 0.0179 mL, 0.120 mmol, 1 eq) was added over 5 minutes at 0° C. in 4 mL of anhydrous ODCB via syringe. The reaction was allowed to warm slowly with stirring overnight to room temperature. The reaction mixture was rotary evaporated to a small volume of ODCB and subjected to chromatography (silica gel, ODCB to elute C₇₀, followed by toluene to collect PC₇₀BM). The PC₇₀BM solution was concentrated to a small volume. PC₇₀BM was then precipitated in methanol and isolated by filtration to obtain 60 mg of material (48% crude yield). The abundance of α-PC₇₀BM (desired product, depicted) was determined to be 95.0% based on NMR analysis. ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.95-7.40 (m, 5H), 3.75 (β, s, 0.08H), 3.68 (a, s, 2.85H), 3.51 (β, s, 0.07H), 2.53-2.40 (m, 4H), 2.27-2.02 (m, 6H). This abundance was qualitatively corroborated by analytical HPLC using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase.

Example 3a di-i-propyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate (3)

To a clean, dry 50 mL round bottom flask was added a stir bar and 1 g (3.69 mmol, 1 eq) of the bromide. The round bottom was sealed and purged three times with inert gas and vacuum. Dichloromethane (4 mL) and diisopropyl sulfide (1.31 g, 1.61 mL, 11.1 mmol, 3 eq) were added to the flask sequentially via syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 15 minutes. Silver tetrafluoroborate (718 mg, 3.69 mmol, 1 eq) was added and the reaction was stirred for 4 hours while warming to room temperature slowly. During this time, the reaction was kept in the dark. Dichloromethane was added and the reaction was extracted twice with water. The DCM layer was dried with magnesium sulfate, filtered, and solvent was removed by rotary evaporation. The crude product was taken up in ethyl acetate and loaded onto a small column which was then flushed with copious ethyl acetate to remove impurities. Product was then eluted with acetone. The acetone was removed by rotary evaporation and a small amount of DCM was added to precipitate silica gel that had come through with the acetone. The DCM was filtered to remove silica gel and once again the solution was rotary evaporated to dryness. 500 mg of product was obtained (34% yield). ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.6-7.3 (m, 5H), 5.37 (dd, J=5.5 Hz, J=17.0 Hz, 0.1H), 4.94 (t, J=12.8 Hz, 0.9H), 4.12 (septet, J=11.5 Hz, 0.9H), 3.64 (s, 3H), 3.14 (septet, J=11.5 Hz, 0.9H), 2.99 (septet, J=11.1 Hz, 0.2H), 2.8-1.0 (m, 6H), 1.76 (d, J=11.5 Hz, 3H), 1.70 (d, J=11.5 Hz, 3H), 1.43 (d, J=11.5 Hz, 3H), 1.24 (d, J=11.5 Hz, 3H).

Example 3b [6,6]-Phenyl C₇₁ butyric acid methyl ester

To a clean, dry 500 mL round bottom flask was added a stir bar and 955 mg (1.136 mmol, 1 eq) of C₇₀. The round bottom was sealed and purged three times with inert gas and vacuum. 220 mL of ODCB (1,2-dichlorobenzene) anhydrous solvent was added by cannula. Sulfonium salt (3) (450 mg, 1.136 mmol, 1 eq) was taken into 20 mL of anhydrous ODCB and added to the reaction by syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 30 minutes. DBU (1,8-diazabicyclo[5.4.0]undec-7-ene, 0.170 mL, 1.136 mmol, 1 eq) was added dropwise over 10 minutes at 0° C. in 20 mL of anhydrous ODCB via syringe. The reaction was allowed to warm slowly to room temperature and stir over 3 days. The reaction mixture was rotary evaporated to a small volume of ODCB and subjected to chromatography (silica gel, ODCB used to elute C₇₀, followed by increasing ratio of toluene to ODCB to collect PC₇₀BM). The PC₇₀BM solution was concentrated to dryness and dissolved in a small volume of toluene. The PC₇₀BM solution was then subjected to high pressure sodium lamp irradiation in order to convert minor amounts of [5,6] adduct to [6,6] adduct. A small amount of PC₆₀BM impurity was then removed by preparative intermediate pressure liquid chromatography using a column with Cosmosil PBB material as the stationary phase (from Nacalai Tesque; pentabromobenzyl group bonded silica) and toluene as the mobile phase. The collected material was then further purified by preparative intermediate pressure liquid chromatography using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase. Fractions containing pure product were combined. The solution was concentrated to a small volume. PC₇₀BM was then precipitated in methanol and isolated by filtration to obtain 250 mg of material (21% yield). The sample was left in an oven overnight at 70° C. under reduced pressure to remove residual solvent. α-PC₇₀BM (desired product, depicted) was obtained exclusively, based on NMR analysis. ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.95-7.40 (m, 5H), 3.68 (a, s, 3.00H), 2.53-2.40 (m, 4H), 2.27-2.02 (m, 6H). β-PC₇₀BM was not detected by regular ¹H NMR, nor was it detected by analytical HPLC using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase.

Example 4a ethyl-i-propyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate (4)

To a clean, dry 50 mL round bottom flask was added a stir bar and 0.5 g (1.84 mmol, 1 eq) of the bromide. The round bottom was sealed and purged three times with inert gas and vacuum. Dichloromethane (2 mL) and isopropyl ethyl sulfide (576.5 mg, 0.698 mL, 5.53 mmol, 3 eq) were added to the flask via syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 40 minutes. Silver tetrafluoroborate (359 mg, 1.84 mmol, 1 eq) was added and the reaction was stirred overnight while warming to room temperature slowly. During this time, the reaction was kept in the dark. Dichloromethane was added and the reaction was extracted twice with water. The DCM layer was dried with magnesium sulfate, filtered, and solvent was removed by rotary evaporation. The crude product was taken up in ethyl acetate, and left in the freezer overnight. It was then loaded onto a small column which was flushed with copious ethyl acetate to remove impurities. Product was then eluted with acetone. The acetone was removed by rotary evaporation and a small amount of DCM was added to precipitate silica gel that had come through with the acetone. The DCM was filtered to remove silica gel and once again the solution was rotary evaporated to dryness. 286 mg of product (6) was obtained (41% yield). ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.6-7.4 (m, 5H), 4.99 (t, J=12.9 Hz, 0.5H), 4.86 (t, J=12.9 Hz, 0.5H), 4.08 (septet, J=11.5 Hz, 0.65H), 3.7-3.4 (m, 3.65H), 3.31 (quintet, J=11.3 Hz, 0.5H), 3.18 (sextet, J=12.0 Hz, 0.6H), 2.98 (sextet, J=12.0 Hz, 0.6H), 2.5-2.1 (m, 4.5H), 1.8-1.2 (m, 9H), 1.01 (t, J=12.5 Hz, 1.5H).

Example 4b [6,6]-Phenyl C₇₁ butyric acid methyl ester

To a clean, dry 50 mL round bottom flask was added a stir bar, 45.5 mg (0.119 mmol, 1 eq) of the sulfonium salt (6) and 100 mg (0.119 mmol, 1 eq) of C₇₀. The round bottom was sealed and purged three times with inert gas and vacuum. 9 mL of ODCB (1,2-dichlorobenzene) anhydrous solvent was added by syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 15 minutes. DBU (1,8-diazabicyclo[5.4.0]undec-7-ene, 0.0178 mL, 0.119 mmol, 1 eq) was added over 5 minutes at 0° C. in 1 mL of anhydrous ODCB via syringe. The reaction was allowed to warm slowly with stirring overnight to room temperature. This abundance of α-PC₇₀BM (desired product, depicted) was qualitatively greater than that obtained from the didodecyl precursor but surprisingly less than that obtained from the methyl isopropyl precursor. α-Isomer abundance was determined by analytical HPLC using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase.

Example 5a didodecyl-(5-methoxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate (5)

To a clean, dry 50 mL round bottom flask was added a stir bar and 0.5 g (1.84 mmol, 1 eq) of the bromide. The round bottom was sealed and purged three times with inert gas and vacuum. Solid isopropyl ethyl sulfide (2.05 g, 5.53 mmol, 3 eq) dissolved in dichloromethane (2 mL) was added to the flask via syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 40 minutes. The reaction mixture was observed to freeze. Silver tetrafluoroborate (359 mg, 1.84 mmol, 1 eq) was added and the reaction was stirred overnight while warming to room temperature. During this time, the reaction was kept in the dark. Dichloromethane was added and the reaction was extracted twice with water. The DCM layer was dried with magnesium sulfate, filtered, and solvent was removed by rotary evaporation. The crude product was taken up in ethyl acetate, and left in the freezer overnight. Silica TLC was used to adjust the conditions used for further isolation versus other sulfonium salt examples. Ethyl Acetate was removed by evaporation and the product mixture was redissolved in a 7:3 ratio of cyclohexane and ethyl acetate. This solution was loaded onto a small column which was flushed with copious amounts of a 7:3 ratio of cyclohexane:ethyl acetate to remove impurities. Product was then eluted with ethyl acetate. The ethyl acetate was removed by rotary evaporation to give 884 mg of the desired product (7) (74% yield). ¹H NMR (500 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.6-7.4 (m, 5H), 5.07 (t, J=13.0 Hz, ¹H), 3.63 (s, 3H), 3.52 (octet, J=12.5 Hz, 2H), 3.20 (quintet, J=9.3 Hz, 1H), 2.92 (quintet, J=9.3, Hz, 1H), 2.4-1.0 (m, 46H), 0.88 (t, J=11.5 Hz, 6H).

Example 5b [6,6]-Phenyl C₇₁ butyric acid methyl ester

To a clean, dry 50 mL round bottom flask was added a stir bar, 77.2 mg (0.119 mmol, 1 eq) of the sulfonium salt (7) and 100 mg (0.119 mmol, 1 eq) of C₇₀. The round bottom was sealed and purged three times with inert gas and vacuum. 9 mL of ODCB (1,2-dichlorobenzene) anhydrous solvent was added by syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 15 minutes. DBU (1,8-diazabicyclo[5.4.0]undec-7-ene, 0.0178 mL, 0.119 mmol, 1 eq) was added over 5 minutes at 0° C. in 1 mL of anhydrous ODCB via syringe. The reaction was allowed to warm slowly with stirring overnight to room temperature. This abundance of α-PC₇₀BM (desired product, depicted) was qualitatively similar to the product mixture that is obtained from the more traditional tosylhydrazone precursor (˜85%). α-Isomer abundance was determined by analytical HPLC using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase.

Example 6a Hexyl 5-phenylpentanoate

An oil bath was preheated to 40° C. To a clean, dry 2 L round bottom flask was added a stir bar, 0.84 L of deionized water, 35.2 mL (280 mmol, 2 eq) of hexanol, 4.32 mL of DBSA (4-dodecylbenzenesulfonic acid mixture of isomers, 14 mmol, 0.1 eq), and 25 g (140 mmol, 1 eq) of phenyl valeric acid. The mixture was allowed to stir at 40° C. for 3 days. The reaction was cooled, quenched with saturated aqueous sodium bicarbonate, and extracted 3× with ethyl acetate. The combined ethyl acetate layer was dried with magnesium sulfate, filtered, and solvent was removed by rotary evaporation. Excess hexanol was removed from the product by rotary evaporation at 65° C. and high vacuum. To remove DBSA, the remaining oil was diluted with a mixture of cyclohexane and ethyl acetate in a 19:1 ratio and run through a plug of silica gel using a mixture of cyclohexane and ethyl acetate in a 19:1 ratio as eluent. The product band was collected and concentrated to constant weight to give 32.05 g (87.1% yield) of product as a near colorless oil. ¹H NMR (300 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.31-7.13 (m, 5H), 4.05 (t, J=6.7 Hz, 2H), 2.63 (t, J=7.1 Hz, 2H), 2.32 (t, J=7.9 Hz, 2H), 1.74-1.53 (m, 6H), 1.40-1.21 (m, 6H), 0.89 (t, J=6.7 Hz, 3H).

Example 6b Hexyl 5-phenyl-5-bromopentanoate

An oil bath was preheated to 85° C. To a clean, dry 1 L round bottom flask was added a stir bar, 32.05 g of the starting material (122 mmol, 1 eq), 23.91 g of NBS (134 mmol, 1.1 eq) and 87.5 mg of benzoyl peroxide (0.361 mmol, 0.003 eq). The flask was fitted with a condenser, sealed, pump purged 3× with inert gas and vacuum, and anhydrous cyclohexane (329 mL) was added by cannula. The mixture was allowed to stir and reflux over two nights. The reaction was cooled, filtered, rinsed with cyclohexane, and rotary evaporated to constant weight to give a quantitative yield of product as a light orange oil. ¹H NMR (300 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.42-7.23 (m, 5H), 4.95 (t, J=7.5 Hz, 1H), 4.05 (t, J=6.8 Hz, 2H), 2.38-2.09 (m, 4H), 1.93-1.52 (m, 4H), 1.40-1.19 (m, 6H), 0.88 (t, J=6.7 Hz, 3H).

Example 6c di-i-propyl-(5-hexyloxy-5-oxo-1-phenylpentyl) sulfonium tetrafluoroborate

To a clean, dry 50 mL round bottom flask was added a stir bar and 2 g (5.86 mmol, 1 eq) of the brominated starting material. The round bottom was sealed and purged three times with inert gas and vacuum. Anhydrous acetonitrile (6.36 mL) and diisopropyl sulfide (2.08 g, 2.55 mL, 17.6 mmol, 3 eq) were added to the flask sequentially via syringe. The reaction was cooled to 0° C. and allowed to equilibrate for 15 minutes. Silver tetrafluoroborate (1.141 g, 5.86 mmol, 1 eq) was added and the reaction was stirred overnight while warming to room temperature (the bath was removed after the addition). The reaction was kept in the dark. The crude reaction mixture was filtered and rinsed with acetonitrile to remove solid silver byproduct. The filtrate was concentrated to an oil by rotary evaporation. The crude product was taken up in a mixture of cyclohexane and ethyl acetate (7:3 ratio) and loaded onto a plug of silica. The plug was flushed with copious amount of a mixture of cyclohexane and ethyl acetate (9:1 ratio), followed by 100% ethyl acetate, followed by acetone. Less polar impurities were removed by the less polar eluent. The desired product was found in the ethyl acetate and acetone fractions. The combined solvents were removed by rotary evaporation and a small amount of DCM was added to precipitate silica gel that had come through with the acetone. The DCM was filtered to remove silica gel and once again the solution was rotary evaporated to dryness. 1.287 g of product was obtained (47.1% yield). ¹H NMR (300 MHz, CDCl₃ (set to 7.26 ppm)) δ 7.55-7.20 (m, 5H), 5.37 (dd, J=3.4 Hz, J=9.4 Hz, 0.15H), 4.88 (dd, J=5.6 Hz, J=9.8 Hz, 0.85H), 4.20-3.95 (m, 2.85H), 3.41 (septet, J=6.9 Hz, 0.85H), 3.22 (septet, J=6.5 Hz, 0.3H), 2.4-2.1 (m, 4H), 1.75 (d, J=6.8 Hz, 3H), 1.7-1.2 (m, 10H), 1.69 (d, J=6.9 Hz, 3H), 1.43 (d, J=7.0 Hz, 3H), 1.21 (d, J=6.93 Hz, 3H), 0.87 (t, J=6.7 Hz, 3H).

Example 6d [6,6]-Phenyl C₇₁ butyric acid hexyl ester

To a clean, dry 100 mL round bottom flask was added a stir bar, 0.6 g of sulfonium salt (1.286 mmol, 1 eq) by pipette, 1.08 g of C₇₀ (1.286 mmol, 1 eq) and 54.1 mL of reagent grade ODCB (1,2-dichlorobenzene). The round bottom was sealed and purged three times with inert gas and vacuum. DBU (1,8-diazabicyclo[5.4.0]undec-7-ene, 0.192 mL, 1.286 mmol, 1 eq) was added dropwise over 45 minutes. The reaction was allowed to stir at room temperature overnight. The reaction mixture was rotary evaporated to ˜25 mL of ODCB and subjected to chromatography (silica gel, ODCB used to elute C₇₀, followed by increasing ratio of toluene to ODCB to collect PC₇₀BM). The PC₇₀BM solution was concentrated to dryness and dissolved in a small volume of toluene (˜100 mL). The PC₇₀BM solution was then subjected to high pressure sodium lamp irradiation for 10 minutes at room temperature (except for any small heating resulting from the irradiation) to convert a minor amount of [5,6] adduct to [6,6] adduct. Solvent was once again removed by rotary evaporation and replaced with 40 mL of toluene. The material was then further purified in one injection by preparative intermediate pressure liquid chromatography using a column with Cosmosil Buckyprep material as the stationary phase (from Nacalai Tesque; pyrenylpropyl group bonded silica) and toluene as the mobile phase. The fraction containing pure product was collected. The solution was concentrated to a small volume. PC₇₀BM was then precipitated in methanol and isolated by filtration. The sample was left in an oven overnight at 70° C. under vacuum to remove residual solvent. α-PC₇₀BC6 (desired product, depicted) was obtained (323 mg, 23% yield) based on HPLC and NMR analysis, which is shown in FIGS. 3 and 5. ¹H NMR (300 MHz, CDCl₃ (set to 7.26 ppm)) δ 8.00-7.30 (m, 5H), 4.06 (alpha, t, J=6.8 Hz, 2H), 2.55-2.35 (m, 6H), 2.30-1.95 (m, 2H), 1.70-1.50 (m, 2H), 1.40-1.15 (m, 6H), 0.89 (t, J=6.8 Hz, 3H). As in can be seen in FIG. 4, a very pronounced decrease of the shoulder reflecting the β-PC₇₀BC6 in the HPLC chromatogram in comparison to the conventional tosylhydrazone method has occurred. Due to the low concentration of β-PC70BC6 and the limited resolution of the chromatogram, no meaningful integration, necessary to quantify the relative abundances, could be conducted despite our best efforts. Similarly, as shown in FIGS. 3 and 5, only very small peaks representing β-PC₇₀BC6 could be observed in the ¹H NMR spectrum, not allowing for a quantitative assessment. Based on HPLC and ¹H NMR, the isomer-selectivity of the synthesis described here, could be demonstrated convincingly.

Unless otherwise defined, used or characterized herein, terms that are used herein (including technical and scientific terms) are to be interpreted as having a meaning that is consistent with their accepted meaning in the context of the relevant art and are not to be interpreted in an idealized or overly formal sense unless expressly so defined herein.

Although the terms, first, second, third, etc., may be used herein to describe various elements, these elements are not to be limited by these terms. These terms are simply used to distinguish one element from another. Thus, a first element, discussed below, could be termed a second element without departing from the teachings of the exemplary embodiments. Spatially relative terms, such as “above,” “below,” “left,” “right,” “in front,” “behind,” and the like, may be used herein for ease of description to describe the relationship of one element to another element, as illustrated in the figures. It will be understood that the spatially relative terms, as well as the illustrated configurations, are intended to encompass different orientations of the apparatus in use or operation in addition to the orientations described herein and depicted in the figures. For example, if the apparatus in the figures is turned over, elements described as “below” or “beneath” other elements or features would then be oriented “above” the other elements or features. Thus, the exemplary term, “above,” may encompass both an orientation of above and below. The apparatus may be otherwise oriented (e.g., rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly. Further still, in this disclosure, when an element is referred to as being “on,” “connected to,” “coupled to,” “in contact with,” etc., another element, it may be directly on, connected to, coupled to, or in contact with the other element or intervening elements may be present unless otherwise specified.

The terminology used herein is for the purpose of describing particular embodiments and is not intended to be limiting of exemplary embodiments. As used herein, singular forms, such as “a” and “an,” are intended to include the plural forms as well, unless the context indicates otherwise.

It will be appreciated that while a particular sequence of steps has been shown and described for purposes of explanation, the sequence may be varied in certain respects, or the steps may be combined, while still obtaining the desired configuration. Additionally, modifications to the disclosed embodiment and the invention as claimed are possible and within the scope of this disclosed invention.

As such, those skilled in the art will appreciate that the conception, upon which this disclosure is based, may readily be utilized as a basis for the designing of other structures, methods, and systems for carrying out the several purposes of the disclosed subject matter. It is important, therefore, that the claims be regarded as including such equivalent constructions insofar as they do not depart from the spirit and scope of the disclosed subject matter.

Although the disclosed subject matter has been described and illustrated in the foregoing exemplary embodiments, it is understood that the present disclosure has been made only by way of example, and that numerous changes in the details of implementation of the disclosed subject matter may be made without departing from the spirit and scope of the disclosed subject matter, which is limited only by the claims which follow. 

The invention claimed is:
 1. A method of making [6,6]-Phenyl C₇₁ butyric acid ester comprising: reacting fullerene C₇₀ with a dialkyl sulfonium salt having the formula:

where R₁ and R₂ are independently —CR₄R₅R₆; where R₄, R₅, and R₆ are independently selected from H, or alkyl; where for any one of R₁ and R₂ no more than one of R₄, R₅, and R₆ can be H; where R₃ is selected from H, optionally substituted C1-C12 aliphatic wherein one or more carbon CH₂ units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or —NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon CH₂ units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl; where R_(a) is independently selected from H, optionally substituted C1-C6 aliphatic; optionally substituted C3-C6 cycloaliphatic or optionally substituted phenyl; and where X is an anion selected from Br⁻, I⁻, Cl⁻, F⁻, BF₄ ⁻, PF₆ ⁻, SbF₆ ⁻, AsF₆ ⁻, OSO₂CH₃ ⁻, OSO₂CF₃ ⁻, OSO₂C₄F₉ ⁻, OSO₂OCH₃ ⁻, OCOCH₃ ⁻, OCOCF₃ ⁻, OSO₂(C₆H₄)CH₃ ⁻, OSO₂(C₆H₄)CF₃ ⁻, N(SO₂CF₃)₂ ⁻, OSO₂CH₂CH₂CH₂CH₂SO₂O⁻, OH⁻, I₃ ⁻, N(CN)₂ ⁻, 7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonate, B(C₆H₅)₄ ⁻ or OSO₂OH⁻ to provide a [6,6]-Phenyl C₇₁ butyric acid ester (C₇₀-PCBR₃) comprising greater than 97 wt % of the α-isomer.
 2. The method of claim 1, wherein one of R₄, R₅, and R₆ is H.
 3. The method of claim 1, wherein R₁ and R₂ are both iso-propyl.
 4. The method of claim 1, wherein R₁ and R₂ are both sec-butyl.
 5. The method of claim 1, wherein R₁ is iso-propyl and R₂ is sec-butyl.
 6. The method of claim 1, wherein R₃ is selected from H and C1-C12 alkyl.
 7. The method of claim 6, wherein R₃ is branched or straight C1-C6 alkyl.
 8. The method of claim 6, wherein R₃ is branched or straight C6 alkyl.
 9. The method of claim 6, wherein R₃ is n-hexyl.
 10. The method of claim 6, wherein one or more carbon CH₂ units of R₃, including terminal carbon, are optionally and independently replaced by —O—.
 11. The method of claim 1, wherein R₃ is a glycolyl.
 12. The method of claim 1, wherein X is BF₄ ⁻.
 13. The method of claim 1, wherein the reaction provides greater than 97.5% selectivity of the α-isomer.
 14. The method of claim 1, wherein the reaction provides greater than 98 wt % selectivity of the α-isomer.
 15. The method of claim 1, wherein reacting comprises reacting the fullerene C70 and the dialkyl sulfonium salt in the presence of a base.
 16. The method of claim 15, wherein the base comprises an organic base.
 17. The method of claim 16 the base comprises 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).
 18. A compound of the formula

comprising greater than 98% of the α-isomer, wherein R₃ is selected from H, optionally substituted C1-C12 aliphatic wherein one or more carbon CH₂ units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or —NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon CH₂ units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl.
 19. A compound of the formula

comprising greater than 99% of the α-isomer, wherein R₃ is selected from H, optionally substituted C1-C12 aliphatic wherein one or more carbon CH₂ units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or —NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon CH₂ units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl.
 20. A compound of the formula

comprising greater than 97% of the α-isomer, wherein R₃ is selected from H, optionally substituted C1-C12 aliphatic wherein one or more carbon CH₂ units, including terminal carbon, are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, thiophenyl, phenyl, pyridinyl or NR_(a)—; optionally substituted C3-C12 cycloaliphatic wherein one or more carbon CH₂ units are optionally and independently replaced by —O—, —S—, carbonyl (—C═O), —CF₂—, or NR_(a); or optionally substituted aryl. 